MicroRNAs and their delivery in diabetic fibrosis

Adv Drug Deliv Rev. 2022 Mar:182:114045. doi: 10.1016/j.addr.2021.114045. Epub 2021 Nov 9.

Abstract

The global prevalence of diabetes mellitus was estimated to be 463 million people in 2019 and is predicted to rise to 700 million by 2045. The associated financial and societal costs of this burgeoning epidemic demand an understanding of the pathology of this disease, and its complications, that will inform treatment to enable improved patient outcomes. Nearly two decades after the sequencing of the human genome, the significance of noncoding RNA expression is still being assessed. The family of functional noncoding RNAs known as microRNAs regulates the expression of most genes encoded by the human genome. Altered microRNA expression profiles have been observed both in diabetes and in diabetic complications. These transcripts therefore have significant potential and novelty as targets for therapy, therapeutic agents and biomarkers.

Keywords: Chronic kidney disease; Diabetes; Fibrosis; Nanotechnology; Noncoding RNA; microRNA; microRNA-based therapeutics.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Biomarkers
  • Diabetes Complications / drug therapy
  • Diabetes Complications / physiopathology
  • Diabetic Nephropathies / drug therapy*
  • Diabetic Nephropathies / physiopathology*
  • Drug Carriers*
  • Fibrosis / drug therapy
  • Fibrosis / physiopathology
  • Humans
  • Hypoglycemic Agents / pharmacology
  • Inflammation / metabolism
  • MicroRNAs / administration & dosage
  • MicroRNAs / pharmacology*
  • MicroRNAs / therapeutic use*
  • Nanoparticle Drug Delivery System

Substances

  • Biomarkers
  • Drug Carriers
  • Hypoglycemic Agents
  • MicroRNAs
  • Nanoparticle Drug Delivery System